Species-Conserved SYNGAP1 Phenotypes Associated with Neurodevelopmental Disorders

SYNGAP1 loss-of-function variants are causally associated with intellectual disability, severe epilepsy, autism spectrum disorder and schizophrenia. While there are hundreds of genetic risk factors for neurodevelopmental disorders (NDDs), this gene is somewhat unique because of the frequency and pen...

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Xehetasun bibliografikoak
Argitaratua izan da:Mol Cell Neurosci
Egile Nagusiak: Kilinc, Murat, Creson, Thomas, Rojas, Camilo, Aceti, Massimiliano, Ellegood, Jacob, Vaissiere, Thomas, Lerch, Jason P., Rumbaugh, Gavin
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2018
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6128754/
https://ncbi.nlm.nih.gov/pubmed/29580901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2018.03.008
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